UniProt | Protein Name |
---|---|
Q9Y5P6 |
|
GO Term | Evidence Code | PMID |
---|---|---|
protein glycosylation | ||
GDP-mannose biosynthetic process |
GO Term | Evidence Code | PMID |
---|---|---|
mannose-1-phosphate guanylyltransferase (GTP) activity | ||
GTP binding | ||
protein binding |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:0050214 | Lambert-Eaton myasthenic syndrome | |
DOID:0050557 | congenital muscular dystrophy | |
DOID:0050559 | Fukuyama congenital muscular dystrophy | |
DOID:0050560 | Walker-Warburg syndrome | |
DOID:0050572 | cone-rod dystrophy | |
DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | |
DOID:0050700 | cardiomyopathy | |
DOID:0060249 | scoliosis | |
DOID:0060255 | rippling muscle disease 2 | |
DOID:0060260 | ptosis |
HPO ID | HPO Term |
---|---|
HP:0001558 | Decreased fetal movement |
HP:0001562 | Oligohydramnios |
HP:0001608 | Abnormality of the voice |
HP:0001638 | Cardiomyopathy |
HP:0001657 | Prolonged QT interval |
HP:0001763 | Pes planus |
HP:0002058 | Myopathic facies |
HP:0002079 | Hypoplasia of the corpus callosum |
HP:0002085 | Occipital encephalocele |
HP:0002093 | Respiratory insufficiency |
Disease ID | Disease Name |
---|---|
ORPHA:363623 |
|
ORPHA:370968 |
|
ORPHA:370959 |
|
OMIM:615351 |
|
OMIM:615350 |
|
ORPHA:353327 |
|
ORPHA:588 |
|
OMIM:615352 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
100689938 | ORENI59621 | ||
115583970 | SPAAU41798 | ||
447346 | Xenbase:XB-GENE-922662 | ||
100037186 | Xenbase:XB-GENE-6255238 | ||
493267 | Xenbase:XB-GENE-922650 | ||
101934259 | CHRPI24410 | ||
109318261 | CROPO25358 | ||
113454477 | PSETE02832 | ||
103816951 | SERCA11185 | ||
100397938 | CALJA11912 |
GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024